Work

Novel SCN1A mutation in the IFMT motif of the α1 subunit of the voltage-gated NaV1.1 channel causing familial hemiplegic migraine

Year: 2013

Type: article

Abstract: Familial hemiplegic migraine (FHM) is a monogenic subtype of migraine with aura. So far three FHM genes are identified; the CACNA1A gene, the ATP1A2 gene and the SCN1A gene.

Source: The Journal of Headache and Pain

DOI: 10.1186/1129-2377-14-s1-p19

Authors: B De Vries, CM Weller, O De Fàbregues, SC Koelewijn, AH Stam, J Haan, MD Ferrari, GM Terwindt, AMJ van den Maagdenberg

Institutions: Leiden University Medical Center, Corporació Sanitària Parc Taulí

Language: English

Topic: Migraine and Headache Studies

Subfield: Psychiatry and Mental health

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: gold

Estimated APC paid: $3,990

OpenAlex ID: W1963697803

FWCI: 0.237

Cites:

Cited by: 1

Related to: 10